Apoptosis induction in HL-60 cells and inhibition of topoisomerase II by triterpene celastrol

被引:101
|
作者
Nagase, M
Oto, J
Sugiyama, S
Yube, K
Takaishi, Y
Sakato, N
机构
[1] Kagawa Univ, Fac Agr, Dept Life Sci, Miki, Kagawa 7610795, Japan
[2] Kagawa Med Univ, Res Equipment Ctr, Miki, Kagawa 7610793, Japan
[3] Univ Tokushima, Fac Pharmaceut Sci, Tokushima 7708505, Japan
[4] Ehime Univ, United Grad Sch Agr Sci, Matsuyama, Ehime 7908566, Japan
关键词
celastrol; derivative; apoptosis; topoisomerase II; HL-60; cells;
D O I
10.1271/bbb.67.1883
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Celastrol, which is a triterpene purified from Celastraceae plants, has anticancer and anti-inflammatory activities. In this study we investigated to clarify whether celastrol can induce apoptosis in a human leukemia HL-60 model system. Celastrol was found to induce apoptosis, and the rank order of the potency of celastrol and its derivatives to induce internucleosomal DNA fragmentation was found to be celastrol > cela-H much greater than the other derivatives = vehicle control. Many anticancer agents are known to possess the ability to inhibit topoisomerase II, so the inhibitory activities of celastrol and its derivatives on topoisomerase II were also explored. The rank order of the inhibitory activity was found to be celastrol>etoposide>cela-H, indicating that the apoptosis-inducing activities of cela derivatives correspond to their inhibitory activities on topoisomerase II. These data suggested that celastrol may cause its effects such as anticancer activity by the mechanism of apoptosis along with topoisomerase II inhibition.
引用
收藏
页码:1883 / 1887
页数:5
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